1. A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity. (7th June 2019) Authors: Bradfield, Jonathan P; Vogelezang, Suzanne; Felix, Janine F; Chesi, Alessandra; Helgeland, Øyvind; Horikoshi, Momoko; Karhunen, Ville; Lowry, Estelle; Cousminer, Diana L; Ahluwalia, Tarunveer S; Thiering, Elisabeth; Boh, Eileen Tai-Hui; Zafarmand, Mohammad H; Vilor-Tejedor, Natalia; Wang, Carol A... Journal: Human molecular genetics Issue: Volume 28:Number 19(2019) Page Start: 3327 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Assessing causal links between metabolic traits, inflammation and schizophrenia: a univariable and multivariable, bidirectional Mendelian-randomization study. (31st August 2019) Authors: Lin, Bochao D; Alkema, Anne; Peters, Triinu; Zinkstok, Janneke; Libuda, Lars; Hebebrand, Johannes; Antel, Jochen; Hinney, Anke; Cahn, Wiepke; Adan, Roger; Luykx, Jurjen J Journal: International journal of epidemiology Issue: Volume 48:Number 5(2019) Page Start: 1505 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Association of common variants identified by recent genome-wide association studies with obesity in Chinese children: a case-control study. Issue 1 (December 2016) Authors: Wang, Hai-Jun; Hinney, Anke; Song, Jie-Yun; Scherag, André; Meng, Xiang-Rui; Grallert, Harald; Illig, Thomas; Hebebrand, Johannes; Wang, Yan; Ma, Jun Journal: BMC medical genetics Issue: Volume 17:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Common obesity risk alleles in childhood attention‐deficit/hyperactivity disorder1. Issue 4 (26th March 2013) Authors: Albayrak, Özgür; Pütter, Carolin; Volckmar, Anna‐Lena; Cichon, Sven; Hoffmann, Per; Nöthen, Markus M.; Jöckel, Karl‐Heinz; Schreiber, Stefan; Wichmann, H‐Erich; Faraone, Stephen V.; Neale, Benjamin M.; Herpertz‐Dahlmann, Beate; Lehmkuhl, Gerd; Sinzig, Judith; Renner, Tobias J.; Romanos, Marcel; W... Journal: American journal of medical genetics Issue: Volume 162:Issue 4(2013) Page Start: 295 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Cover Image, Volume 171B, Number 6, September 2016. Issue 6 (12th August 2016) Authors: Mooney, Michael A.; McWeeney, Shannon K.; Faraone, Stephen V.; Hinney, Anke; Hebebrand, Johannes; Nigg, Joel T.; Wilmot, Beth Journal: American journal of medical genetics Issue: Volume 171:Issue 6(2016) Page Start: i Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Decreased melanocortin‐4 receptor function conferred by an infrequent variant at the human melanocortin receptor accessory protein 2 gene. Issue 9 (30th July 2016) Authors: Schonnop, Laura; Kleinau, Gunnar; Herrfurth, Nikolas; Volckmar, Anna‐Lena; Cetindag, Cigdem; Müller, Anne; Peters, Triinu; Herpertz, Stephan; Antel, Jochen; Hebebrand, Johannes; Biebermann, Heike; Hinney, Anke Journal: Obesity Issue: Volume 24:Issue 9(2016) Page Start: 1976 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Detailed stratified GWAS analysis for severe COVID-19 in four European populations. Issue 23 (15th July 2022) Authors: Degenhardt, Frauke; Ellinghaus, David; Juzenas, Simonas; Lerga-Jaso, Jon; Wendorff, Mareike; Maya-Miles, Douglas; Uellendahl-Werth, Florian; ElAbd, Hesham; Rühlemann, Malte C; Arora, Jatin; Özer, Onur; Lenning, Ole Bernt; Myhre, Ronny; Vadla, May Sissel; Wacker, Eike M; Wienbrandt, Lars; Blandino... Journal: Human molecular genetics Issue: Volume 31:Issue 23(2022) Page Start: 3945 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Exploration of large, rare copy number variants associated with psychiatric and neurodevelopmental disorders in individuals with anorexia nervosa. (August 2017) Authors: Yilmaz, Zeynep; Szatkiewicz, Jin P.; Crowley, James J.; Ancalade, NaEshia; Brandys, Marek K.; van Elburg, Annemarie; de Kovel, Carolien G.F.; Adan, Roger A.H.; Hinney, Anke; Hebebrand, Johannes; Gratacos, Monica; Fernandez-Aranda, Fernando; Escaramis, Georgia; Gonzalez, Juan R.; Estivill, Xavier;... Journal: Psychiatric genetics Issue: Volume 27:Number 4(2017:Aug.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Genetic variation at the CELF1 (CUGBP, elav‐like family member 1 gene) locus is genome‐wide associated with Alzheimer's disease and obesity. Issue 4 (1st May 2014) Authors: Hinney, Anke; Albayrak, Özgür; Antel, Jochen; Volckmar, Anna‐Lena; Sims, Rebecca; Chapman, Jade; Harold, Denise; Gerrish, Amy; Heid, Iris M.; Winkler, Thomas W.; Scherag, André; Wiltfang, Jens; Williams, Julie; Hebebrand, Johannes; GERAD Consortium; IGAP Consortium; GIANT Consortium Journal: American journal of medical genetics Issue: Volume 165:Issue 4(2014) Page Start: 283 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. High-throughput DNA methylation analysis in anorexia nervosa confirms TNXB hypermethylation. (3rd April 2018) Authors: Kesselmeier, Miriam; Pütter, Carolin; Volckmar, Anna-Lena; Baurecht, Hansjörg; Grallert, Harald; Illig, Thomas; Ismail, Khadeeja; Ollikainen, Miina; Silén, Yasmina; Keski-Rahkonen, Anna; Bulik, Cynthia M.; Collier, David A.; Zeggini, Eleftheria; Hebebrand, Johannes; Scherag, André; Hinney, Anke Journal: World journal of biological psychiatry Issue: Volume 19:Number 3(2018) Page Start: 187 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗